NZ252604A - Use of hexaflumuron and similar compounds for controlling termites - Google Patents
Use of hexaflumuron and similar compounds for controlling termitesInfo
- Publication number
- NZ252604A NZ252604A NZ252604A NZ25260493A NZ252604A NZ 252604 A NZ252604 A NZ 252604A NZ 252604 A NZ252604 A NZ 252604A NZ 25260493 A NZ25260493 A NZ 25260493A NZ 252604 A NZ252604 A NZ 252604A
- Authority
- NZ
- New Zealand
- Prior art keywords
- wood
- termites
- fluoro
- chloro
- timber
- Prior art date
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/34—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B27—WORKING OR PRESERVING WOOD OR SIMILAR MATERIAL; NAILING OR STAPLING MACHINES IN GENERAL
- B27K—PROCESSES, APPARATUS OR SELECTION OF SUBSTANCES FOR IMPREGNATING, STAINING, DYEING, BLEACHING OF WOOD OR SIMILAR MATERIALS, OR TREATING OF WOOD OR SIMILAR MATERIALS WITH PERMEANT LIQUIDS, NOT OTHERWISE PROVIDED FOR; CHEMICAL OR PHYSICAL TREATMENT OF CORK, CANE, REED, STRAW OR SIMILAR MATERIALS
- B27K3/00—Impregnating wood, e.g. impregnation pretreatment, for example puncturing; Wood impregnation aids not directly involved in the impregnation process
- B27K3/34—Organic impregnating agents
- B27K3/38—Aromatic compounds
- B27K3/40—Aromatic compounds halogenated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S424/00—Drug, bio-affecting and body treating compositions
- Y10S424/11—Termite treating
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Health & Medical Sciences (AREA)
- Forests & Forestry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Saccharide Compounds (AREA)
- Catching Or Destruction (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
- External Artificial Organs (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Method of using specific acyl urea compounds as termiticides. The compounds are unusually non-repellant to termites and active at low dosages.
Description
<div class="application article clearfix" id="description">
<p class="printTableText" lang="en">New Zealand Paient Spedficaiion for Paient Number £52604 <br><br>
252 6 0 4 <br><br>
New Zealand No. 252604 International No. PCT/US93/04569 <br><br>
TO BE ENTERED AFTER ACCEPTANCE AND PUBUCATION <br><br>
Priority dates; 11 I ^'2- <br><br>
Intemational filing date: <br><br>
Classification: RoirJi+f/34; <br><br>
fcon K3|tfo <br><br>
Publication date: 2 5 JUN 1996 Journal No J (l+oS. <br><br>
NEW ZEALAND PATENTS ACT 1953 <br><br>
COMPLETE SPECMCATTON <br><br>
; <br><br>
Title of invention: <br><br>
Novel use of hexaflumuron and related compounds as termiticides <br><br>
Name, address and nationality of ' <br><br>
upplicant(s) as in international application form: <br><br>
DOWELANCO, 9330 Zionsville Road, Indianapolis, <br><br>
Indiana 46268, United States of Americafa Co <br><br>
\xn.atr -Hva.to.wg oP <br><br>
# <br><br>
\ lovy <br><br>
252 6 0 4 <br><br>
P 93/24011 PCT/US93/04569 <br><br>
lot <br><br>
NOVEL USE OF HEXAFLUMURON AND RELATED COMPOUNDS AS TERMITICIDES <br><br>
BACKGROUND OF THE INVENTION <br><br>
Termites, insects of the order Isoptera, live almost exclusively on cellulose in vegetable matter. However, they can cause considerable damage to other materials in their quest for cellulose, including 5 structural damage to buildings, destruction of foods such as growing crops, grassland, forestry (especially young saplings), household goods, stored food, cellulose based materials such as wood, paper, cotton, fiber matter, and the like. The tendency to attack 10 each of the above materials will vary from species to species. <br><br>
Damage to structures or other materials may be prevented or diminished by the use of insecticidal compounds active against termites. Such compounds are 15 conventionally applied either to the termite infested material itself or to its component members, e.g., by treatment of timber components before incorporation of the timber into the building, or to soil area surrounding the building. <br><br>
20 The majority of commercially available insecticides do not have the combination of biological and physicochemical properties necessary for effective termite control (e.g., activity against termites <br><br>
252 6 0 4 <br><br>
•> 93/24011 <br><br>
PCT/US93/04569 <br><br>
2 <br><br>
combined with long-term persistence), although the chlorinated hydrocarbon aldrin has proved effective. <br><br>
However, increased regulatory controls on chlorinated hydrocarbons have created a need for a 5 termiticide which combines the necessary activity and persistence with a low mammalian toxicity. <br><br>
Certain acyl urea compounds are claimed to be effective against termites. For instance, U.S. Patent No. 4,833,158 claims flufenoxuron as a termiticide; 10 and diflubenzuron has also been disclosed specifically as a termiticide. <br><br>
Hexaflumuron (N-(((3,5-dichloro-4-(1,1,2,2-tetra-fluoroethoxy)phenyl)amino)carbonyl)-2,6-difluoro benzazmide), a compound with a low mammalian toxicity, 15 has been described as possessing insecticidal activity against insects from the orders Lepidoptera, Coleoptera, Diptera, Orthoptera, Homoptera, Thysanoptera, and Acarina (U.S. Patent No. 4,468,405). It has now been found that hexaflumuron and other structurally related 20 compounds are surprisingly more effective as a termiticide than structurally unrelated acyl urea compounds such as, for instance, diflubenzuron. <br><br>
The present invention provides a method for 25 treating a locus for termites which comprises applying to the locus a compound of the formula <br><br>
DESCRIPTION OF THE INVENTION <br><br>
FORMULA I <br><br>
2 5 2S04 <br><br>
03 93/24011 PCT/US93/04569 <br><br>
3 <br><br>
wherein Ri and R2 are each independently hydrogen, C1-C3 alkyl or C1-C3 alkoxy, chloro, brorno or fluoro; <br><br>
Xi and X2 are each independently chloro, fluoro, <br><br>
bromo, hydrogen or C1-C3 alkyl; and R is a fluorine 5 containing C1-C4 haloalkoxy group. <br><br>
Processes for preparation of the compounds of Formula I are readily available. <br><br>
The advantage and surprising effect of the use of a compound of Formula I as a termiticide lies in 10 its efficacy at surprisingly low doses and its unique non-repellant effect on termites even at high concentrations. Known methods of termite treatment necessitate the use of relatively large amounts of termiticide to create a physical barrier of relatively 15 high chemical concentrations sufficient to kill some insects and deter others from immediately reinfesting the treated locus by causing those termites to move to an untreated location. The present invention effectively eliminates termite populations by allowing 20 a large number of termites to actually visit, contact and carry away a small but efficacious amount of the nonrepellant, termiticidal compound. <br><br>
In order to facilitate the application of the compounds of Formula I to the desired locus, or to 25 facilitate storage, transport or handling, the compound is normally formulated with a carrier and/or a surface-active agent. <br><br>
A carrier in the present context is any material with which the compound of Formula I (active ingredient) 30 is formulated to facilitate application to the locus, or storage, transport or handling. A carrier may be a solid or a liquid, including a material which is normally gaseous but which has been compressed to form a liquid. Any of the carriers normally used or known <br><br>
252 6 0 4 <br><br>
b 93/24011 PCT/US93/04569 <br><br>
4 <br><br>
to be usable in formulating insecticidal compositions may be used. <br><br>
Compositions according to the invention contain 0.0001 to 99.9% by weight active ingredient. <br><br>
5 Preferably, compositions according to the invention contain 0.001 to 10.0% by weight of active ingredient though proportions as low as 0.0001% may be useful in some circumstances. <br><br>
Suitable solid carriers include natural and 10 synthetic clays and silicates, for example natural silicas such as diatomaceous earths; magnesium silicates, for example talcs; magnesium aluminium silicates, for example attapulgites and vermiculites; aluminium silicates, for example kaolinites, 15 montmorillonites and micas; calcium carbonate; calcium sulphate; ammonium sulphate; synthetic hydrated silicon oxides and synthetic calcium or aluminium silicates; elements, for example carbon and sulfur; <br><br>
natural and synthetic resins, for example coumaronne 20 resins, polyvinyl chloride, and styrene polymers and copolymers; solid polychlorophenols; bitumen; waxes; <br><br>
agar; and solid fertilizers, for example superphosphates. Cellulose based materials, for example wood, sawdust, agar or Methocel®, as well as the 25 other solid carriers that are themselves attractive to or at least non-repellant to termites are particularly suitable and preferable. Mixtures of different solids are often suitable. For example, a mixture of wood flour and agar formulated as a moisture containing 30 solid would be preferable. <br><br>
Suitable liquid carriers include water; <br><br>
alcohols, for example isopropanol and glycols; <br><br>
ketones, for example acetone, methyl ethyl ketone, <br><br>
methyl isobutyl ketone, isophorone and cyclohexanone; 35 ethers; aromatic or aliphatic hydrocarbons, for <br><br>
25 2 G 0 <br><br>
#) 93/24011 PCT/US93/04569 <br><br>
5 <br><br>
example benzene, toluene and xylene; petroleum fractions, for example kerosene and light mineral oils; chlorinated hydrocarbons, for example carbon tetrachloride, perchloroethylene and trichloroethane; <br><br>
5 polar organic liquids, such as dimethyl formamide, <br><br>
dimethyl acetamide, dimethyl sulfoxide and N-methyl-pyrrolidone. Mixtures of different liquids are often suitable, for example a mixture of isophorone with a polar organic solvent such as N-methylpyrrolidone, as 10 are mixtures of solid and liquid carriers. <br><br>
Pesticidal compositions are often formulated and transported in a concentrated form which is subsequently diluted by the user before application. The presence of small amounts of a carrier which is a 15 surface-active agent facilitates this process of dilution. Thus it is suitable to use at least one carrier in such a composition which is a surfaceactive agent. For example, the composition may contain at least two carriers, at least one of which is a 20 surface-active agent. <br><br>
A surface-active agent may be an emulsifying agent, a dispersing agent or a wetting agent; it may be nonionic or ionic. Examples of suitable surface-active agents include the sodium or calcium salts of 25 polyacrylic acids and lignin sufonic acids; the condensation of fatty acids or aliphatic amines or amides containing at least 12 carbon atoms in the molecule with ethylene oxide and/or propylene oxide; <br><br>
fatty acid esters of glycerol, sorbitol, sucrose or 3 0 pentaerythritol; condensates of these with ethylene oxide and/or propylene oxide; condensates of these with ethylene oxide and/or propylene oxide; <br><br>
condensation products of fatty alcohol or alkyl phenols, for example p-octylphenol or p-octylcresol, 35 with ethylene oxide and/or propylene oxide; sulfates or sulfonates of these condensation products; alkali <br><br>
252 6 0 4 <br><br>
•> 93/24011 PCT/US93/04569 <br><br>
6 <br><br>
or alkaline earth metal salts, preferably sodium salts, or sulfuric or sulfonic acid esters containing at least 10 carbon atoms in the molecule, for example sodium lauryl sulphate, sodium secondary alkyl 5 sulfates, sodium salts of sulfinated castor oil, and sodium alkylaryl sulfonates such as dodecylbenzene sulfonate; and polymers of ethylene oxide and copolymers of ethylene oxide and propylene oxide. <br><br>
Pesticidal compositions may for example be 10 formulated as wettable powders, dusts, granules, <br><br>
baits, solutions, emulsifiable concentrates, <br><br>
emulsions, suspension concentrates and aerosols. <br><br>
Wettable powders usually contain 25, 50 or 75% <br><br>
weight of active ingredient and usually contain in 15 addition to solid inert carrier, 3-10% weight of a dispersing agent and, where necessary, 0-10% weight of stabilizer(s) and/or other additives such as penetrants or stickers. <br><br>
Dusts are usually formulated as a dust concentrate 20 having a similar composition to that of a wettable powder but without a dispersant, and are diluted in the field with further solid carrier to give a composition usually containing 0.5-10% weight of active ingredient. <br><br>
25 Granules are usually prepared to have a size between 10 and 100 BS mesh (1.676-0.152 mm), and may be manufactured by, for example, agglomeration or impregnation techniques. Generally, granules will contain 0.01-75% weight active ingredient and 0-10% 3 0 weight of additives such as stabilizers, surfactants, <br><br>
slow release modifiers and binding agents. The so-called "dry flowable powders" consist of relatively, <br><br>
small granules having a relatively high concentration of active ingredient. Of particular interest in <br><br>
25 2 0 0 <br><br>
) 93/24011 PCT/US93/04569 <br><br>
7 <br><br>
current practice are the water dispersible granular formulations. These are in the form of dry, hard granules that are essentially dust-free, and are resistant to attrition on handling, thus minimizing 5 the formation of dust. On contact with water, the granules readily disintegrate to form stable suspensions of the particles of active material. Such formulation contain 90% or more by weight of finely divided active material, 3-7% by weight of a blend of 10 surfactants, which act as wetting dispersing, <br><br>
suspending and binding agents, and 1-3% by weight of a finely divided carrier, which acts as a resuspending agent. <br><br>
Baits are prepared by, for example, combining a 15 mixture of a finely divided cellulose material, such as sawdust, with an amount of active ingredient sufficient to provide the desired result; for example, <br><br>
from about 0.001% to about 20% weight active ingredient and forming the mixture into a paste by the 20 addition of about 1% to 5% of a water based binder such as agar. The paste-like mixture is packed into a housing such as a hollowed out wooden dowel. Baits are a preferable embodiment of the present invention. <br><br>
Wood or timber is impregnated with active 25 ingredient according to well known procedures including pressure treatments such as the Lowery empty cell process and full cell process, vacuum treatments, hot and cold bath treatment, thermal treatment, and cold-soak treatment. Surface treatment of wood or 30 timber is accomplished by well known techniques such as brushing, dipping, spraying or short-soaking the wood material with active ingredient or appropriate compositions thereof in amounts and in a manner that would be apparent to one skilled in the art. <br><br>
35 For instance, wood treatments may be <br><br>
25 2 6 0 4 <br><br>
|0 93/24011 PCT/US93/04569 <br><br>
8 <br><br>
accomplished by two major methods: impregnation of the wood through vacuum and pressure treatments and surface treatments such as painting, spraying or dipping. In an impregnation method, a concentrate may 5 be formulated which contains 1-65% weight per volume active ingredient, 5-50% solvent and, when necessary, co-solvent, and 0-20% w/v of other additives such as penetrants. For treatment, vacuum is pulled on a vessel containing the wood. The concentrate is then 10 added to the vessel and subsequently pressurized to force concentrate into the wood. The vessel is relieved of pressure and the treated wood then removed. In a surface treatment, the concentrate may be simply painted onto a wood surface by means of 15 brushing or spraying or, preferably, dipping. <br><br>
Solvents used for these types of treatments may include polyethylene glycol, and aromatic solvents, <br><br>
and the like due to their ability to penetrate wood. <br><br>
Emulsifiable concentrates usually contain, in 20 addition to a solvent and, when necessary, co-solvent, 10-50% weight per volume active ingredient, 2-20% <br><br>
weight per volume emulsifiers and 0-20% weight per volume of other additives such as stabilizers, <br><br>
penetrants and corrosion inhibitors. <br><br>
25 Suspension concentrates are usually compounded so as to obtain a stable, non-sedimenting flowable product and usually contain 10-75% weight active ingredient, 0.5-15% weight of dispersing agents, 0.1-10% weight of suspending agents such as protective 30 colloids and thixotropic agents, 0-10% weight of other additives such as defoamers, corrosion inhibitors, stabilizers, penetrants and stickers, and water or an organic liquid in which the active ingredient is substantially insoluble; certain organic solids or .35 inorganic salts may be present dissolved in the formulation to assist in preventing sedimentation or <br><br>
2 5 2 6 0 4 <br><br>
93/24011 PCT/US93/04569 <br><br>
9 <br><br>
as anti-freeze agents for water. <br><br>
Aqueous dispersions and emulsions are compositions which may be obtained by diluting a wettable powder or a concentrate with water. The said emulsions may be 5 of the water-in-oil or of the oil-in-water type, and may have a thick 'mayonnaise'-like consistency. <br><br>
Termiticidal compositions may also contain other ingredients, for example further active compounds possessing herbicidal, insecticidal or fungicidal 10 properties, in accordance with the requirement of the locus to be treated and the treatment method. <br><br>
The method of applying a compound of Formula I to combat termites comprises applying the compound, conveniently in a composition comprising the compound of 15 Formula I and a carrier as described above, to a locus or area to be treated for the termites, such as soil or timber, already subject to infestation or attack by termites or intended to be protected from infestation by termites. The active ingredient is, of course, applied 20 in an amount sufficient to effect the desired action of combatting termite infestation. This dosage is dependent upon many factors, including the carrier employed, the method and conditions of the application, whether the formulation is present at the locus in the 25 form of a film, or as discrete particles or as a bait, the thickness of film or size of particles, the degree of termite infestation, and the like. <br><br>
Proper consideration and resolution of these factors to provide the necessary dosage of the active 30 ingredient at the locus to be protected are within the skill of those versed in the art. In general, however, the effective dosage of the compound of the invention at the locus to be protected--i.e., the dosage to which the termite has access—is of the order of 0.001 <br><br>
252 6 0 4 <br><br>
93/24011 PCT/US93/04569 - <br><br>
10 <br><br>
to 1.0% based on the total weight of the composition, <br><br>
though under some circumstances the effective concentration may be as little as 0.0001% or as much as 2%, on the same basis. <br><br>
5 In one embodiment of this invention, the compounds of Formula I are used to combat termites in the soil, thereby achieving indirect protection for any timberbased constructions erected on the treated soil or to crops, grassland, forestry (especially 10 young saplings), and other cellulose based materials surrounded by or located in the treated soil. <br><br>
Suitable soil-based control of termites is obtained by providing in the soil a termiticidaly effective dosage of a compound of Formula I. For use in this manner, 15 the active ingredient is suitably applied to the soil at a rate of from about. 0.01 gram to about 10 kilograms per hectare. Depending on the composition used, good control of soil inhabiting termites is obtained at rates of from about 0.01 gram to about 1 20 kilogram per hectare and preferably from about 0.1 gram to 100 grams per hectare. The compound of Formula I can conveniently be formulated for use as a compound--impregnated wooden stake, bait, granule or powder containing a solid diluent, or as a suspension 25 concentrate. Such formulation usually contain from about 0.001 to about 50% by weight of the compound. <br><br>
Effective control results when the formulation is physically integrated into the topsoil as well as when it is applied to the surface of the soil. <br><br>
?0 The compound of formula I can also be applied as a drench--that is, as a solution or dispersion of the compound in a suitable solvent or liquid diluent. <br><br>
Such drenches can.be prepared by diluting with water a concentrate containing the compound of Formula I, an 35 emulsifying agent, and preferably an organic solvent, <br><br>
such as isophorone and/or N-methylpyrrolidone. The <br><br>
252 6 04 <br><br>
3 93/24011 PCT/US93/04569 - <br><br>
11 <br><br>
compound of formula I can be applied by band, furrow or side-dress techniques, and may be incorporated or not. <br><br>
In another embodiment of the invention, compounds of 5 Formula I are applied directly on or into the material to be protected or treated. For example, timber is treated either before, during or after its incorporation into a structure or building, thereby protecting it against damage from termite attack or combating an 10 already existing infestation of termites. For treatment of timber, the composition may contain a penetrant designed to facilitate penetration of the active ingredient to a significant depth in the timber, thereby ensuing that superficial surface abrasion will not 15 generate a surface free from active ingredient and thus vulnerable to termite penetration. <br><br>
Examples of materials known for use as wood penetrants include paraffinic hydrocarbons, for instance low aromatic white spirit, 2-ethoxyethanol and methyl 20 isobutyl ketone. Preferably the penetrant is <br><br>
2-ethoxyethanol or methyl isobutyl ketone, optionally in association with isophorone and/or N-methyl pyrrolidone. <br><br>
It is useful in such timber treatment to incorporate "anti-bloom" agent, which counteract the tendency for 25 the active ingredient to migrate to the surface <br><br>
("blooming"), suitable materials being dibutyl phthalate and o-dichlorobenzene. <br><br>
Timber treatment compositions may also, if desired, contain fungicides (to prevent fungal attacks 30 such as. dry rot and wet rot), and/or pigments in order to combine termite protection with painting of the timber. In this context, painting will be understood to include.not only the application of covering pigmentation (commonly white), but also the 3 5 application of natural wood coloration in order to <br><br>
2 5 2 6 0 4 <br><br>
93/24011 PCTVUS93/04569 <br><br>
12 <br><br>
restore the appearance of weathered timber (e.g., as with treatments to red cedar external housing timbers). <br><br>
The actual application onto or into the timber 5 may be carried out using conventional techniques including immersion of the timber in the liquid, <br><br>
painting the liquid onto -the timber by spray or brushing, and injecting the liquid into the timber. <br><br>
The concentration of active ingredient in the 10 treated timber should, of course, be sufficient to achieve desired termiticidal effect. However, the total volume of formulated product taken up by the timber is limited by the absorption properties of the wood with respect to that formulation and will also 15 vary according to the application procedure adopted (immersing, painting or injecting); hence the concentration of active ingredient in the formulation should be such as to produce the desired concentration in the treated timber. The formulation may be 20 aqueous, as for example obtained by dilution of a conventional insecticide emulsifiable concentrate, or non-aqueous such as an undiluted emulsifiable concentrate. The organic solvent in such formulations will suitably be one of those previously described. <br><br>
25 The determination of the necessary parameters applicable to specific types of wood and particular treatment procedures can readily be determined by established techniques conventionally used by those skilled in the art. In general, however, the 30 effective dosage of the compound in the wood may be as low as 0.1 ppm, with the maximum dosage dictated by cost considerations rather than biological efficacy. <br><br>
The invention is illustrated in the following examples: <br><br>
Example 1 : Comparative efficacv q£_ hexaf lumuron <br><br>
93/24011 <br><br>
SM dif lubenzuron <br><br>
13 <br><br>
PCT/US93/04569 <br><br>
252 6 <br><br>
A unit comprised a screw-top glass jar (6.0 cm diam. by 6.5 cm high) in which two 8 cm3 wood (Pinus spp. ) cubes were placed 1.5 cm apart,- covered with 75 5 cm3 0f acetone-washed sand and moistened with 18 ml of deionized water. One wood cube was previously treated with an acetone solution of hexafluniuron or dif lubenzuron at concentrations ranging from 1 to 1000 ppm (wt/vol). <br><br>
One hundred workers (undifferentiated larvae of 10 at least third instar) plus five soldiers of formosanus were placed in each experimental unit. Termites were previously collected from three field colonies. Units were held at 28 ±1 °C. After 6 and 9 weeks, three units per treatment were disassembled, 15 the surviving termites counted and ecdysis inhibitory effects on termites were recorded. Treatments were replicated three times per sample interval with each replicate representing a different termite colony. The results are summarized in Table I. <br><br>
93/24011 <br><br>
252 6 0 4 <br><br>
PCT/US93/04569 <br><br>
1A <br><br>
Table I <br><br>
Percent Mortality of £Lu ,£grm<?gflnus (+ standard error) <br><br>
Concentration 6 weeks 9 weeks <br><br>
(ppm) #1 #2 #1 #2 <br><br>
0 <br><br>
15 <br><br>
.0 <br><br>
± <br><br>
2 <br><br>
.4 <br><br>
17 .3 <br><br>
+ <br><br>
8 <br><br>
.3 <br><br>
16 <br><br>
.3 <br><br>
± <br><br>
1 <br><br>
.9 <br><br>
26 <br><br>
.0 <br><br>
± <br><br>
11. <br><br>
,5 <br><br>
7 . <br><br>
8 <br><br>
66 <br><br>
.5 <br><br>
+ <br><br>
12 <br><br>
.5 <br><br>
22, <br><br>
.7 <br><br>
± <br><br>
4 <br><br>
.7 <br><br>
80 <br><br>
.3 <br><br>
± <br><br>
9 <br><br>
.3 <br><br>
34 <br><br>
.3 <br><br>
+ <br><br>
4. <br><br>
.3 <br><br>
15. <br><br>
6 <br><br>
65 <br><br>
.0 <br><br>
+ <br><br>
4 <br><br>
.2 <br><br>
15 <br><br>
.0 <br><br>
± <br><br>
7 <br><br>
.8 <br><br>
87 <br><br>
.8 <br><br>
+ <br><br>
8 <br><br>
.4 <br><br>
27 <br><br>
.7 <br><br>
+ <br><br>
14. <br><br>
.2 <br><br>
31. <br><br>
3 <br><br>
68 <br><br>
.3 <br><br>
± <br><br>
7 <br><br>
.4 <br><br>
18, <br><br>
.3 <br><br>
± <br><br>
5 <br><br>
.8 <br><br>
92 <br><br>
.3 <br><br>
± <br><br>
7 <br><br>
.5 <br><br>
44 <br><br>
.7 <br><br>
+ <br><br>
27. <br><br>
.7 <br><br>
62. <br><br>
5 <br><br>
78 <br><br>
.0 <br><br>
-u <br><br>
6 <br><br>
.1 <br><br>
17, <br><br>
.3 <br><br>
6 <br><br>
.9 <br><br>
100 <br><br>
.0 <br><br>
+ <br><br>
0 <br><br>
22 <br><br>
.0 <br><br>
4. <br><br>
.5 <br><br>
125 . <br><br>
0 <br><br>
86 <br><br>
.7 <br><br>
+ <br><br>
3 <br><br>
.9 <br><br>
18 <br><br>
.0 <br><br>
+ <br><br>
5 <br><br>
.0 <br><br>
100 <br><br>
.0 <br><br>
+ <br><br>
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26 <br><br>
. 0 <br><br>
+ <br><br>
4 <br><br>
.7 <br><br>
250. <br><br>
0 <br><br>
84 <br><br>
.8 <br><br>
+ <br><br>
4 <br><br>
.1 <br><br>
18.7 <br><br>
+ <br><br>
5 <br><br>
.2 <br><br>
99 <br><br>
.7 <br><br>
± <br><br>
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.3 <br><br>
45 <br><br>
.0 <br><br>
+ <br><br>
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0 <br><br>
80 <br><br>
.7 <br><br>
+ <br><br>
3 <br><br>
.5 <br><br>
23 <br><br>
.3 <br><br>
± <br><br>
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.7 <br><br>
99 <br><br>
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.3 <br><br>
50 <br><br>
.7 <br><br>
+ <br><br>
24. <br><br>
.7 <br><br>
1000 <br><br>
.0 <br><br>
92 <br><br>
.0 <br><br>
+ <br><br>
3 <br><br>
.1 <br><br>
35 <br><br>
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17 <br><br>
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.0 <br><br>
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.3 <br><br>
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.2 <br><br>
#1 is Hexaflumuron and #2 is Diflubenzuron <br><br>
5 This data demonstrates the surprisingly and significantly greater efficacy of hexaflumuron versus diflubenzuron. After 6 weeks, mortality ranged from 65-92% following exposure to hexaflumuron, compared to 15-35% mortality following exposure to diflubenzuron. <br><br>
10 Only hexaflumuron induced high mortality of 99-100% <br><br>
compared to the highest mortality of 52% after 9 weeks exposure to 1000 ppm diflubenzuron. <br><br>
Example 2: Efficacy of bait containing hexaflumuron against C. formosanus and R. flavines <br><br>
15 Cellulose powder (pulverized sawdust of southern yellow pine, Pinus sp.) was impregnated with acetone solution of hexaflumuron at concentrations of 0; 31.3; 62.5; 125; 500; 1000; 2000; 4000; and 8000 ppm (wt active ingredientjdry wt bait) for flavioes and 0; <br><br>
2 5 2 6 0 4 <br><br>
H> 93/24011 PCT/D593/04569 <br><br>
15 <br><br>
125; 250; 500; 1000; 200.0; 4000; 8000 and 16,000 ppm for formosanus. Water and agar solution were added to the dry cellulose powder to yield a bait matrix that contained 78% water and 2% agar. The experimental 5 units were comprised of screw-top glass jars (6.0 cm diam. by 6.5 cm high) in which two plastic containers (1.9 cm diam by 2.4 cm high) were placed about 1 cm apart and covered with 75 ml acetone washed sand and 18 ml deionized water. Eight holes (0.238 cm ID) were 10 predrilled on the side of the plastic container about 0.5 cm from the bottom to allow termite entry. One container contained treated bait, the other contained untreated bait matrix. The wet weight of bait placed in each plastic container was determined before use. 15 Twenty seven units were prepared for each concentration. One hundred workers (plus 10 soldiers for SLl. formosanus and one soldier for fL. flavipes) <br><br>
were placed in each unit and held at 28 ±1 "C. For each termite species, the test was replicated nine 20 times using termites collected from three colonies at three different dates. Nine units per treatment were disassembled at 3, 6, and 9 weeks. The number of surviving termites and those with, molting inhibitory effects were counted. The remaining bait was 25 extracted from the plastic container and reweighed. Differences in bait consumption between treated and untreated bait were compared by a paired £. test. <br><br>
93/24011 <br><br>
252 6 0 4 <br><br>
PCT/US93/04569 <br><br>
16 <br><br>
Eastern Sub. Termite <br><br>
C <br><br>
o <br><br>
100 80 60 AO <br><br>
JD. <br><br>
t— <br><br>
C <br><br>
■— 20 ir <br><br>
OjO <br><br>
c <br><br>
100 r <br><br>
L <br><br>
so o <br><br>
s <br><br>
60 <br><br>
40 <br><br>
• « <br><br>
20 <br><br>
f—* <br><br>
< <br><br>
G3 <br><br>
% <br><br>
0 <br><br>
f <br><br>
O <br><br>
100 <br><br>
80 <br><br>
c <br><br>
<D <br><br>
60 <br><br>
O <br><br>
AO <br><br>
0 <br><br>
a. <br><br>
20 <br><br>
: Mortality 3 Week : Molting Inhibition <br><br>
1 <br><br>
6 Week <br><br>
T - <br><br>
T T <br><br>
T <br><br>
9 Week <br><br>
10 100 1000 10000 <br><br>
Concentration (pDm) <br><br>
i> 93/24011 <br><br>
252604 <br><br>
PCT/ US93/04569 <br><br>
17 <br><br>
J <br><br>
q m <br><br>
o c <br><br>
<D O <br><br>
(D n <br><br>
Formosan Sub. Termite <br><br>
100 80 •50 40 20 <br><br>
C 100 f <br><br>
3 Week • : Mortality <br><br>
: Moltins Inhibition <br><br>
10 100 1000 10000 <br><br>
Concentration (ppm) <br><br>
252 6 0 4 <br><br>
0)93/24011 PCT/ US93/04569 <br><br>
18 <br><br>
These results demonstrate that even at the lowest concentrations (31.3 ppm and 62.5 ppm for E^. flavipes and 125 ppm for £Lu formosanus) termites acquired a sufficient dose of hexaflumuron to exhibit molting 5 inhibition at 6 weeks and mortality at 9 weeks. These results suggest that the threshold concentration for molting inhibition and lethality is low (probably <10 ppm for B_t_ flavipes and <100 ppm for SL. formosanus) . <br><br>
The concentration threshold for feeding 10 deterrence is high: >4000 ppm and >8000 ppm for E^. <br><br>
flavipes and formosanus. respectively. <br><br>
Example 3: Hexaflumuron bait composition <br><br>
Hexaflumuron 0.1% w/v <br><br>
Sawdust 30.0% <br><br>
15 MethocelR 1.0% <br><br>
Water 68.9% <br><br>
Example 4: Efficacy of .field bait containing hexaflumuron <br><br>
Pine or spruce sawdust was impregnated with an 20 acetone solution of hexaflumuron to yield concentrations of 500-5,000 ppm (dry wt Al/dry wt sawdust) <br><br>
upon evaporation of acetone. The bait matrix was composed of 20% treated sawdust and 80% of agar or MethocelR solution (2%). A bait station was composed 25 of a plastic tubing (2.9 cm diam. I.D. ky 16.5 cm high, one end closed, the other end open) filled with approximately 80 g of bait matrix. Six rows of holes (0.238 mm diam) <br><br>
were pre-drilled on the side of the tubing. <br><br>
Baits were placed into the ground where termites 30 of the species E^. flavipes or formosanus were known to be foraging, and were checked monthly for amount bait matrix consumed. <br><br>
A. Termite infestation of rionr and door frame in Plantation. FL.: Three baits were introduced in <br><br>
252 6 0 4 <br><br>
D 93/24011 PCT/US93/04569 <br><br>
19 <br><br>
February 1991. By April 1991, no termite activity was found in the vicinity. A total of 26 g of bait matrix was consumed; amount of active ingredient consumed was 3.87 mg. Due to absence of termite activity since 5 that time, it is concluded that the entire colony of over 400,000 termites was eliminated by the consumption of 3.87 mg of hexaflumuron within two months. <br><br>
B. Termite infestation in trees and fallen logs, Plantation. FL: Eleven baits were introduced in April <br><br>
10 1991. In June 1991, no termites were detected in the area. During the three months (April - June), 122 g bait matrix/20 mg AI was consumed to eliminate a colony of approximately 730,000 EL. flavipes termites. <br><br>
C. Structural termite infestation In Plantation, 15 Eli: Structural infestation of R. flavipes colony persisted in a two-story apartment building (approx 1,500m2) since 1987. Residents reported annual spring swarniing from the structure for five consecutive years despite annual traditional termiticide treatments 20 since 1986. Following the introduction of 27 baits in August 1991, the termite activity was reduced to 0.1 g/bait/day in September 1991. More baits were placed. By November 1991, no termite activity was detected. <br><br>
During the four month period (August - December), a 25 total of 69 baits were used from which 2,997 g bait matrijc/1,539 mg AI was consumed by the EL. f lavipes colony to eliminate over 2.5 million termites. <br><br>
D. Structural termite infestation In Plantation. FL: Despite repeated soil termiticide treatments and <br><br>
30 a fumigation following the discovery of structural infestations by formosanus in a high rise in 1987, <br><br>
foraging activity remained strong throughout 1989 and 1991. Activity of this colony did not decline even in winter months. Eight baits were introduced in May 35 1991, and over 90% of the bait matrix were consumed <br><br></p>
</div>
Claims (5)
1. A method for treating a locus for termites which comprises applying to a locus a compound of the formula<br><br>
R, X,<br><br>
5 wherein Ri and R2 are each independently hydrogen, C1-C3 alkyl or C1-C3 alkoxy, chloro, bromo or fluoro; Xi and X2 are each independently chloro, fluoro, bromo, hydrogen or C1-C3 alkyl; and R is a fluorine containing C1-C4 haloalkoxy group.<br><br>
10
2. A method of claim 1 wherein said locus comprises soil or timber.<br><br>
3. A method of claim 2 wherein Ri is fluoro or chloro; R2 is hydrogen, fluoro or chloro and R is OCF3, OCF2CHF2; OCF2CHC1F, OCF2CFHBr; OCF2CHFC1;<br><br>
15 OCFClCHFCl; or OCF2CHCI2.<br><br>
4. A method of claim 3 wherein Xi and X2 are CI; Rl is F or Cl; R2 is F or H and R is OCF2CHF2, OCF2CHFC1 or OCF2CHFBr.<br><br>
x-
5. A method of claim 4 wherein Ri and R2 are<br><br>
' 20 both F and R is OCF2CHF2.<br><br>
25 2 6 0<br><br>
o. A method of claim 2 •.•.•herein said soil or -imber is created with a composition comprising the compound and a carrier.<br><br>
7 . a method of claim 6 v/herein Ri is fluoro or 5 chloro; R2 is hydrogen, fluoro or chloro and R is OCF3, OCF2CHF2; OCF2CHC1F, CCF2CFHBr; OCF2CHFC1; OCFC1CHFC1; or OCF2CHCI2•<br><br>
8. A method of claim 7 v/herein Xi and X2 are Cl; Rl is F or Cl; R2 is F or H ana R is OCF2CrfF2, 10 OCF2CHFC1 or OCF2CHFBr.<br><br>
9 . A method of claim 8 wherein Ri and R2 are both F and R is OCF2CHF2.<br><br>
10. A method of ciaim 6 v/herein said carrier comprises wood.<br><br>
11. A method, for treating a locus for termites, as defined in claim 1 substantially as herein described with reference to any example thereof.<br><br>
I ents<br><br>
1<br><br>
-20-<br><br>
</p>
</div>
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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US89161092A | 1992-06-01 | 1992-06-01 |
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NZ252604A NZ252604A (en) | 1992-06-01 | 1993-05-12 | Use of hexaflumuron and similar compounds for controlling termites |
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US (2) | US5556883A (en) |
EP (1) | EP0643561B1 (en) |
JP (1) | JP2866894B2 (en) |
KR (1) | KR100232245B1 (en) |
CN (1) | CN1073801C (en) |
AT (1) | ATE161143T1 (en) |
AU (1) | AU660821B2 (en) |
BR (1) | BR9306460A (en) |
CA (1) | CA2136985C (en) |
DE (1) | DE69315834T2 (en) |
EG (1) | EG21019A (en) |
ES (1) | ES2110606T3 (en) |
GR (1) | GR3026290T3 (en) |
IL (1) | IL105809A (en) |
MX (1) | MX9303230A (en) |
MY (1) | MY111745A (en) |
NZ (1) | NZ252604A (en) |
PH (1) | PH30424A (en) |
TR (1) | TR27505A (en) |
TW (1) | TW282393B (en) |
WO (1) | WO1993024011A1 (en) |
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DE4303012A1 (en) * | 1993-02-03 | 1994-08-04 | Desowag Materialschutz Gmbh | Agent for protecting technical materials, in particular wood and wood-based materials |
WO1995016354A1 (en) * | 1993-12-15 | 1995-06-22 | Ciba-Geigy Ag | Method of combating termites and other wood destructive insects |
DE4409039A1 (en) * | 1993-12-21 | 1995-06-22 | Bayer Ag | Antifouling agents |
US5536501A (en) * | 1994-12-30 | 1996-07-16 | Proguard, Inc. | Use of flavenoid aldehydes as insecticides and for killing arachnids |
FR2742024B1 (en) * | 1995-12-08 | 2001-02-16 | Centre Nat Rech Scient | METHOD OF DESTRUCTION OF DUMMY |
ZA973309B (en) * | 1996-05-01 | 1997-11-14 | Fmc Corp | Method for controlling termites. |
EP0935641A4 (en) * | 1996-10-30 | 2001-12-12 | Tarren Wood Products Inc | Method of pressure treating boards |
US5886221A (en) * | 1997-11-03 | 1999-03-23 | Dow Agrosciences Llc | Benzoylphenylurea insecticides and methods of using certain benzoylphenylureas to control cockroaches, ants, fleas, and termites |
AU5100498A (en) * | 1996-11-08 | 1998-05-29 | Dowelanco Llc | New benzoylphenylurea insecticides and methods of using them to control cockroaches, ants, fleas, and termites |
AU5163698A (en) * | 1996-11-08 | 1998-05-29 | Dowelanco Llc | New benzoylphenylurea insecticides ans methods of using them to control cockroaches |
US5945453A (en) * | 1996-11-08 | 1999-08-31 | Dow Agrosciences Llc | Benzoylphenylurea insecticides to control cockroaches |
WO1998019542A1 (en) * | 1996-11-08 | 1998-05-14 | Dow Agrosciences Llc | New benzoylphenylurea insecticides and methods of using certain benzoylphenylureas to control cockroaches, ants, fleas, and termites |
ES2168741T3 (en) * | 1997-02-12 | 2002-06-16 | Dow Agrosciences Llc | SYNERGIC THERMITICIDE COMPOSITIONS CONTAINING AN INHIBITOR OF THE SYNTHESIS OF THE CHYTIN AND JUVENOIDS. |
MY115581A (en) | 1997-04-15 | 2003-07-31 | Dow Agrosciences | Improved methods and appratus for monitoring or controlling pests |
US5811461A (en) * | 1997-10-31 | 1998-09-22 | Dow Agrosciences Llc | Benzoylphenylurea insecticides and methods of using them to control cockroaches, ants, fleas, and termites |
MY138864A (en) * | 1999-07-05 | 2009-08-28 | Nihon Nohyaku Co Ltd | Ant controllers and method for application thereof |
US6237305B1 (en) * | 2000-01-10 | 2001-05-29 | Phillip G. Landers | Process for in-situ treatment of wood poles |
US6824787B2 (en) | 2000-12-22 | 2004-11-30 | The United States Of America As Represented By The Secretary Of Agriculture | Urea and nitrogen based compounds as feeding stimulants/aggregants and masking agents of unpalatable chemicals for subterranean termites |
TWI301400B (en) * | 2002-02-22 | 2008-10-01 | Ishihara Sangyo Kaisha | Composition for controlling house insect pest and method for controlling house insect pest |
ES2431836T3 (en) * | 2003-04-23 | 2013-11-28 | The Procter & Gamble Company | A composition comprising a cationic polymer that enhances surface deposition |
TWI355237B (en) * | 2004-03-29 | 2012-01-01 | Dow Agrosciences Llc | Pesticide compositions |
TW200605784A (en) * | 2004-05-11 | 2006-02-16 | Bayer Environmental Science Sas | Method to fight against insects including the use of hydrocarbon compounds |
EP1632558A1 (en) * | 2004-09-06 | 2006-03-08 | The Procter & Gamble | A composition comprising a surface deposition enhancing cationic polymer |
EP1661978B1 (en) | 2004-11-29 | 2011-03-02 | The Procter & Gamble Company | Detergent compositions |
EP1661977A1 (en) * | 2004-11-29 | 2006-05-31 | The Procter & Gamble Company | Detergent compositions |
US20070123440A1 (en) * | 2005-11-28 | 2007-05-31 | Loughnane Brian J | Stable odorant systems |
BR112015021663A2 (en) * | 2013-03-11 | 2017-07-18 | Dow Agrosciences Llc | systems and methods for pest infestation control of a woody plant |
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US4468405A (en) * | 1981-07-30 | 1984-08-28 | The Dow Chemical Company | Substituted N-aroyl N'-phenyl urea compounds |
DK172687B1 (en) * | 1981-07-30 | 1999-05-31 | Dow Agrosciences Llc | Substituted N-aroyl-N'-phenyl-urea compounds, intermediate for use in the preparation thereof, a process for d. |
CA1238650A (en) * | 1982-03-01 | 1988-06-28 | Hiroshi Nagase | Urea derivatives, their production and use |
DE3217620A1 (en) * | 1982-05-11 | 1983-11-17 | Bayer Ag, 5090 Leverkusen | 2,5-DIHALOGENBENZOYL (THIO) UREA, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PEST CONTROL |
DE3217619A1 (en) * | 1982-05-11 | 1983-11-17 | Bayer Ag, 5090 Leverkusen | 2,4-DIHALOGENBENZOYL (THIO) UREA, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PEST CONTROL |
EP0179021A3 (en) * | 1984-10-18 | 1987-05-13 | Ciba-Geigy Ag | Benzoylphenyl ureas |
GB8700838D0 (en) * | 1987-01-15 | 1987-02-18 | Shell Int Research | Termiticides |
-
1992
- 1992-12-07 TW TW081109790A patent/TW282393B/zh not_active IP Right Cessation
-
1993
- 1993-05-12 JP JP6500579A patent/JP2866894B2/en not_active Expired - Lifetime
- 1993-05-12 CA CA002136985A patent/CA2136985C/en not_active Expired - Fee Related
- 1993-05-12 KR KR1019940704421A patent/KR100232245B1/en not_active IP Right Cessation
- 1993-05-12 AT AT93911309T patent/ATE161143T1/en not_active IP Right Cessation
- 1993-05-12 BR BR9306460A patent/BR9306460A/en not_active IP Right Cessation
- 1993-05-12 EP EP93911309A patent/EP0643561B1/en not_active Expired - Lifetime
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- 1993-05-12 NZ NZ252604A patent/NZ252604A/en unknown
- 1993-05-12 ES ES93911309T patent/ES2110606T3/en not_active Expired - Lifetime
- 1993-05-12 WO PCT/US1993/004569 patent/WO1993024011A1/en active IP Right Grant
- 1993-05-14 TR TR00405/93A patent/TR27505A/en unknown
- 1993-05-25 IL IL105809A patent/IL105809A/en unknown
- 1993-05-26 EG EG32793A patent/EG21019A/en active
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JPH07507307A (en) | 1995-08-10 |
ATE161143T1 (en) | 1998-01-15 |
IL105809A0 (en) | 1993-09-22 |
TR27505A (en) | 1995-06-07 |
MX9303230A (en) | 1993-12-01 |
EP0643561B1 (en) | 1997-12-17 |
CN1073801C (en) | 2001-10-31 |
BR9306460A (en) | 1998-06-30 |
EG21019A (en) | 2000-09-30 |
US5691383A (en) | 1997-11-25 |
KR950701801A (en) | 1995-05-17 |
JP2866894B2 (en) | 1999-03-08 |
WO1993024011A1 (en) | 1993-12-09 |
EP0643561A1 (en) | 1995-03-22 |
AU660821B2 (en) | 1995-07-06 |
PH30424A (en) | 1997-05-09 |
CA2136985A1 (en) | 1993-12-09 |
KR100232245B1 (en) | 1999-12-01 |
DE69315834D1 (en) | 1998-01-29 |
IL105809A (en) | 1998-06-15 |
CA2136985C (en) | 1998-10-06 |
DE69315834T2 (en) | 1998-04-09 |
TW282393B (en) | 1996-08-01 |
AU4248793A (en) | 1993-12-30 |
US5556883A (en) | 1996-09-17 |
ES2110606T3 (en) | 1998-02-16 |
GR3026290T3 (en) | 1998-06-30 |
CN1081318A (en) | 1994-02-02 |
MY111745A (en) | 2000-12-30 |
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